On-Site Pharma Manufacturing Project Manager

LEGAL PROJECT MANAGEMENT PARTNERS LLC; Juncos (PR); On-site; USD 90,000 - 140,000; Full time

Job summary

LEGAL PROJECT MANAGEMENT PARTNERS LLC is seeking an experienced Project Manager to lead capital and operational initiatives in a GMP pharmaceutical manufacturing setting, overseeing projects from initiation to completion.

You will coordinate Manufacturing, Engineering, Quality, Validation, Facilities and Operations, ensuring on-time delivery, compliance, and alignment with business goals.

Qualifications

• Bachelors in Engineering required; Master's is a plus.
• Minimum 5 years of project management in pharma.
• PMP certification preferred; strong leadership abilities.

Responsibilities

• Lead project delivery and governance for GMP pharma initiatives.
• Develop and monitor plans, schedules, budgets, and risks.
• Coordinate cross-functional teams across manufacturing, engineering, quality, validation, facilities, and operations.
• Chair meetings and report status, milestones, and risks to stakeholders.
• Ensure compliance with GMP and company procedures throughout delivery.

Skills

Project management

Stakeholder management

GMP knowledge

Leadership

Communication

Education

Bachelor's in Engineering

Master's in Project Management / Engineering / Business

Tools

Microsoft Office 365

Project management tools

Job description

LEGAL PROJECT MANAGEMENT PARTNERS LLC is seeking an experienced Project Manager to lead capital and operational initiatives in a GMP pharmaceutical manufacturing setting, overseeing projects from initiation to completion.

You will coordinate Manufacturing, Engineering, Quality, Validation, Facilities and Operations, ensuring on-time delivery, compliance, and alignment with business goals.